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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559352Generated: October 29, 2026

HCID 66999754, compound → HCID 66999588, compound

https://huagongshe.com/reaction/559352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66999754HCID 66999754—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 66999588HCID 6699958878.1%

Reaction Steps

A solution of (R)-2-benzyloxymethyl-3-oxo-4-(3-piperidin-1-yl-propyl)-piperazine-1-carboxylic acid tert-butyl ester (321 mg, 0.72 mmol) in acetic acid (9 ml) was stirred for 18 h at room temperature under a hydrogen atmosphere (3 bar) in the presence of palladium (10% on activated charcoal, 161 mg), then insoluble material was removed by filtration and the filtrate evaporated. The residue was partitioned between ethyl acetate and 2 M aq. sodium carbonate solution. The organic layer was dried (MgSO4), filtered, and evaporated to afford the title compound (200 mg, 78%). Light brown oil, MS (ISP)=356.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063042B2
Source datasetuspto-grants-2011_11
ORD IDord-7139270a0dab4e5ca748332abdde5330
Source noteuspto-grants-2011_11